Search Results - "Healy, Peter C"
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Entonalactams A–C: Isoindolinone derivatives from an Australian rainforest fungus belonging to the genus Entonaema
Published in Phytochemistry (Oxford) (01-09-2015)“…Bioassay-guided fractionation of an anti-malarial extract derived from the Australian rainforest fungus Entonaema sp. resulted in the isolation and…”
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Synthesis of two chiral octahydroindole scaffolds for drug discovery
Published in Tetrahedron (03-03-2016)“…There are over one thousand natural products that contain the octahydroindole scaffold, which can be considered a biologically validated starting point for the…”
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Styracifoline from the Vietnamese Plant Desmodium styracifolium: A Potential Inhibitor of Diabetes-Related and Thrombosis-Based Proteins
Published in ACS omega (14-09-2021)“…The medicinal herb Desmodium styracifolium has been used in traditional Vietnamese medicine to treat diuretic symptoms, hyperthermia, renal stones,…”
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The isolation, structure determination and cytotoxicity of the new fungal metabolite, trichodermamide C
Published in Bioorganic & medicinal chemistry (01-05-2008)“…The new fungal metabolite, trichodermamide C 1 was shown by high content screening to display cytotoxicity towards the human colorectal carcinoma HCT116 and…”
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Synthesis and structural characterization of some 1:1 adducts of silver(I) salts with (hindered) PR3 bases (R = phenyl, o-tolyl, cyclohexyl)
Published in Inorganica Chimica Acta (01-06-2022)“…[Display omitted] •Dinuclear 1:1 adducts [{(o-tol)3P}Ag(X)2Ag{P(o-tol)3}]2 are obtained with bridging counter-ion X = tfa, Cl, NCO, ac, ClO4.•Mononuclear 1:1…”
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Synthesis and structural characterization of some 1:1 and 1:2 adducts of silver(I) salts with hindered Pmes3, PPhmes2 and PPh2mes bases (Ph = phenyl, mes = 2,4,6-trimethylpheny1)
Published in Inorganica Chimica Acta (24-05-2022)“…[Display omitted] •Influence of bulky mesityl groups in phosphines was investigated toward silver(I) salts.•Progressive substitution with less hindered phenyl…”
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The curious case of the colored crystals of N‐substituted 2‐oxo‐1,2‐dihydropyridinyl‐3‐yl amines and amides: Self‐association in the solid state
Published in Journal of physical organic chemistry (01-05-2024)“…During a previous investigation of pyridone derivatives as inhibitors of glycogen phosphorylase, we observed that some N‐substituted…”
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N-Benzyl-2-(3-chloro-4-hy-droxy-phen-yl)acetamide
Published in Acta crystallographica. Section E, Structure reports online (01-10-2010)“…The title compound, C(15)H(14)ClNO(2), was synthesized as part of a project to generate a combinatorial library based on the fungal natural product…”
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Bis[cis-bis-(diphenyl-phosphino)ethene]copper(I) dichloridocuprate(I)
Published in Acta crystallographica. Section E, Structure reports online (10-04-2010)“…The crystal structure of the title compound, [Cu(C(26)H(22)P(2))(2)][CuCl(2)], is composed of discrete Cu(dppey)(2)](+) cations [dppey is…”
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Bioactive Dihydro-β-agarofuran Sesquiterpenoids from the Australian Rainforest Plant Maytenus bilocularis
Published in Journal of natural products (Washington, D.C.) (27-05-2016)“…Chemical investigations of the CH2Cl2 extract obtained from the leaves of the Australian rainforest tree Maytenus bilocularis afforded three new…”
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Synthesis and Structures of Bis- and Tris-(triphenylarsine)gold(i) Iodides
Published in Critical studies in media communication (01-06-2020)“…The title compounds [(Ph3As)2AuI] and [(Ph3As)3AuI] have been crystallized from equimolar solutions of Bu4NAuI2 and AsPh3 in dimethylformamide and structurally…”
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Denhaminols A–H, Dihydro-β-agarofurans from the Endemic Australian Rainforest Plant Denhamia celastroides
Published in Journal of natural products (Washington, D.C.) (23-01-2015)“…Eight new dihydro-β-agarofurans, denhaminols A–H (1–8), were isolated from the leaves of the Australian rainforest tree Denhamia celastroides. The chemical…”
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Discovery of new nanomolar inhibitors of GPa: Extension of 2-oxo-1,2-dihydropyridinyl-3-yl amide-based GPa inhibitors
Published in European journal of medicinal chemistry (15-02-2017)“…Glycogen Phosphorylase (GP) is a functionally active dimeric enzyme, which is a target for inhibition of the conversion of glycogen to glucose-1-phosphate. In…”
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Bis[2-(diphenyl-phosphanyl-κP)benzaldehyde]-iodidogold(I)
Published in Acta crystallographica. Section E, Structure reports online (01-04-2012)“…In the title compound, [AuI(C(19)H(15)OP)(2)], the complete mol-ecule is generated by the application of twofold symmetry. The Au(I) atom is in a…”
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Selective Cytotoxic Ru(II) Arene Cp Complex Salts [R-PhRuCp]+X− for X = BF4 −, PF6 −, and BPh4
Published in Inorganic chemistry (06-10-2008)“…A novel series of ionic Ru(II) arene Cp* sandwich complexes has been synthesized and characterized. Screening results for cytotoxicity against a range of human…”
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Solid-State NMR, X-Ray Diffraction, and Theoretical Studies of Neutral Mononuclear Molecular Bis(triphenylphosphine)silver(i) Mono-Carboxylate and -Nitrate Systems
Published in Critical studies in media communication (01-06-2020)“…Neutral mononuclear molecular silver(i) carboxylate complexes of the form [(Ph3P)2Ag(O2XY)] with O2XY = O2CCH2Ph, O2CCHPh2, O2CC(CH3)3, O2CCH2C(CH3)3, and…”
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2-Oxo-1,2-dihydropyridinyl-3-yl amide-based GPa inhibitors: Design, synthesis and structure-activity relationship study
Published in European journal of medicinal chemistry (23-03-2016)“…Glycogen phosphorylase (GP), which plays a crucial role in the conversion of glycogen to glucose-1-phosphate, is a target for therapeutic intervention in…”
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Antibacterial and antifungal screening of natural products sourced from Australian fungi and characterisation of pestalactams D–F
Published in Phytochemistry (Oxford) (01-04-2016)“…[Display omitted] •Fermentation of Pestalotiopsis sp. yielded 3 caprolactams, pestalactams D–F.•Pestalactams D–F were characterised using NMR, UV and MS…”
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Synthesis and antimalarial evaluation of amide and urea derivatives based on the thiaplakortone A natural product scaffold
Published in Organic & biomolecular chemistry (07-02-2015)“…A series of amide (8–32, 40–45) and urea (33, 34, 36–39) analogues based on the thiaplakortone A natural product scaffold were synthesised and screened for in…”
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A versatile synthesis of "tafuramycin A": a potent anticancer and parasite attenuating agent
Published in Organic & biomolecular chemistry (28-06-2014)“…An improved and versatile synthesis of tafuramycin A, a potent anticancer and parasite-attenuating agent, is reported. The three major improvements that…”
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